Evidence map›Paper›PMID 31014367›Full record

ArticleBreast cancer research : BCR2019

The pro- and anti-tumor roles of mesenchymal stem cells toward BRCA1-IRIS-overexpressing TNBC cells.

Daniel Ryan, Bibbin T Paul, Jim Koziol, Wael M ElShamy

Open access · goldAbstract read
In one paragraph

Article in Breast cancer research : BCR, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.2field-weighted citation impact, top 14% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

14 citing papers in PubMed, 24 citations in OpenAlex.

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  12. The Role ofCancers · 2021
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  14. Contralateral breast cancer in patients carrying mutations in the BRCA1∕2 gene.Romanian journal of morphology and embryology = Revue roumaine de morphologie et embryologie
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 3 institutions in 1 country.

Daniel RyanBreast Cancer Program, San Diego Biomedical Research Institute, 10865 Road to Cure, Suite 100, San Diego, CA, 92121, USA.
Bibbin T PaulDepartment of Molecular Biology and Biophysics, University of Connecticut Health Center, Farmington, CT, USA.
Jim KoziolDepartment of Molecular and Experimental Medicine, The Scripps Research Institute, La Jolla, CA, USA.
Wael M ElShamyBreast Cancer Program, San Diego Biomedical Research Institute, 10865 Road to Cure, Suite 100, San Diego, CA, 92121, USA. welshamy@sdbri.org.
San Diego Biomedical Research Institute · USScripps Research Institute · USUConn Health · US

Funding

Bi-directional interactions with tumor microenvironment enhance BRCA1-IRIS overexpressing TNBC tumor cells aggressivenessR01CA194447 · NCI · UNIVERSITY OF MISSISSIPPI MED CTR · PI ELSHAMY, WAEL M. · 2015 to 2019
$1.9M
NCI NIH HHS R01 CA194447
6 · The paper itself

Abstract

backgroundTo evaluate the cross-talk between BRCA1-IRIS (IRIS)-overexpressing (IRISOE) TNBC cells and tumor-resident mesenchymal stem cells (MSCs) that triggers the aggressiveness or elimination of IRISOE TNBC tumors.

methodsWe analyzed the effect of silencing or inactivating IRIS on the bi-directional interaction between IRISOE TNBC cells and MSCs on tumor formation and progression. We analyzed the downstream signaling in MSCs induced by IL-6 secreted from IRISOE TNBC cells. We compared the effect of MSCs on the formation and progression of IRIS-proficient and deficient-TNBC cells/tumors using in vitro and in vivo models. Finally, we analyzed the association between IL-6, PTGER2, and PTGER4 overexpression and breast cancer subtype; hormone receptor status; and distant metastasis-free or overall survival.

resultsWe show high-level IL-6 secreted from IRISOE TNBC cells that enhances expression of its receptor (IL-6R) in MSCs, their proliferation, and migration toward IRISOE, in vitro, and recruitment into IRISOE TNBC tumors, in vivo. In serum-free medium, recombinant IL-6 and the IL-6-rich IRISOE TNBC cell condition media (CM) decreased STAT3

conclusionsThe IL-6/PGE

Indexed as

Alternative SplicingBiomarkers, TumorGene Expression Regulation, NeoplasticAnimalsBRCA1 ProteinCell Line, TumorDinoprostoneDisease Models, AnimalFemaleGene Knockdown TechniquesHumansInterleukin-6Mesenchymal Stem CellsMiceModels, BiologicalPrognosisBiomarkers, TumorBRCA1 ProteinBRCA1 protein, humanDinoprostoneInterleukin-6BRCA1-IRISIL-6Mesenchymal stem cellsMetastasisProstaglandin E2STAT3Triple-negative breast cancer

Identifiers

PMID31014367
PMCPMC6480921
OpenAlexW2946750486

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.